93978-88-2

Upstream product

• 93960-55-5 methyl 3-O-benzoyl-4-O-benzyl-6-bromo-2,6-dideoxy-α-D-ribo-hexopyranoside 
• 93978-82-6 methyl 3-O-benzoyl-4-O-benzyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 93960-56-6 methyl 3-O-benzoyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 62346-15-0 methyl 2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 74-90-8 hydrogen cyanide 
• 124-63-0 methanesulfonyl chloride 
• 93978-85-9 methyl 4-O-benzyl-2,6-dideoxy-β-L-threo-hexopyranosid-3-ulose 
• 172603-41-7 methyl 4-O-benzyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 

Downstream Products

• 94062-88-1 (3S,4S,5S,7S)-4-Benzyloxy-7-methoxy-5-methyl-6-oxa-1-aza-spiro[2.5]octane 
• 75044-07-4 methyl 4-O-benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside 
• 93978-91-7 N-((2S,3S,4R,6S)-3-Benzyloxy-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-yl)-benzamide 

Relevant academic research and scientific papers

Branched-chain sugars. XXXVI. A new synthesis of methyl 4-O-benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside, a derivative of the branched-chain amino sugar of antibiotic A35512B

The compound was synthesized from methyl 4-0-benzyl-2,6-dideoxy- beta -L-threo-hexopyranosid-3-ulose through cyanomesylation, reductive spiro aziridine formation, and reductive ring-opening. When (2-methyoxyethoxymethyl) group was used as the protecting g